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APQP

The document outlines quality management system requirements for suppliers of Powers & Sons. It specifies that suppliers must establish, document, implement, and continually improve their quality management system. The system must identify processes, determine sequences and interactions, and ensure effective operation. It must also ensure availability of resources, monitor processes, implement actions for improvement, and include quality policy statements, a quality manual, procedures, and records. For APQP, suppliers are expected to follow the AIAG manual and use its guidelines. Suppliers must also follow AIAG manuals for FMEAs and control plans. Powers & Sons requires the latest revisions of FMEAs, process flow diagrams, and control plans on file and approved.

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377 views2 pages

APQP

The document outlines quality management system requirements for suppliers of Powers & Sons. It specifies that suppliers must establish, document, implement, and continually improve their quality management system. The system must identify processes, determine sequences and interactions, and ensure effective operation. It must also ensure availability of resources, monitor processes, implement actions for improvement, and include quality policy statements, a quality manual, procedures, and records. For APQP, suppliers are expected to follow the AIAG manual and use its guidelines. Suppliers must also follow AIAG manuals for FMEAs and control plans. Powers & Sons requires the latest revisions of FMEAs, process flow diagrams, and control plans on file and approved.

Uploaded by

danielsasikumar
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Advanced Product Quality Planning (APQP) Section 6

Suppliers shall have a Quality Manual specific to their company explaining The Company Quality System. Each supplier shall establish, document, implement and maintain a quality management system and continually improve its effectiveness. The supplier shall: A) Identify the processes needed for the quality management system and their application throughout the organization. B) Determine the sequence and interaction of these processes. C) Determine criteria and methods needed to ensure that both the operation and control of these processes are effective. D) Ensure the availability of resources and information necessary to support the operation and monitoring of these processes. E) Monitor, measure and analyze these processes. F) Implement actions necessary to achieve planned results and continual improvement of these processes. The Quality Management System shall include: A) Documented statements of a quality policy and quality objectives. B) A Quality Manual. C) Documented procedures necessary to carry out the Quality Management System. D) Documents needed by the supplier to ensure the effective planning, operation and control of its processes. E) Records required as evidence that the Quality System is effective.

APQP: For the APQP process the supplier are expected to follow the AIAG Advanced Product Quality Planning and Control Plan manual (Current Edition). The following is to be used as a guide: 1) 2) 3) 4) 5) 6) 7) 8) Planning and Define program. Product Design and Development. Process Design and Development. Product and Process Validation. Feedback, Assessment and Corrective Action. Control Plan Methodology. Product Quality Planning Checklists. Analytical Techniques.

Section 6-1

SIM 10/1/09

FMEAs: The supplier is expected to follow the AIAG Potential Failure Mode and Effects Annalysis manual (Current Edition), in the development of FMEAs. Process Flow Diagrams: The supplier shall provide a Process Flow Diagram representing the current process flow. The format to be used will be agreed upon between Powers & Sons and the supplier. Control Plans: The supplier is expected to follow the standard practice for Control Plan format. The format is from Advanced Product Quality Planning and Control Plan manual (Current Edition). Requirements: Powers & Sons must have on file the latest revisions for the following documents: 1) FMEAs 2) Process Flow Diagrams 3) Control Plans The FMEAs and the Control Plans must be approved by Powers & Sons. The approved documents must be on file at Powers & Sons. If any changes are made to any of the documents listed above, the document shall be submitted to Powers & Sons for approval. This may require a PPAP resubmission; see Production Part Approval Process manual section I-3 (Current Edition) for resubmission requirements. Note (Waivers): Waiver from the PPAP process must be submitted in writing to Powers & Sons Purchasing Department. The waiver will be approved and / or disapproved and returned to the supplier.

Section 6-2

SIM 10/1/09

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